Soft Whisper Dandruff Shampoo (A.P. Deauville) – Water Specification Fail (2020)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Soft Whisper by Powerstick Dandruff Shampoo (Pyrithione Zinc), 14.4 FL OZ. (426 mL), A.P. Deauville LLC New Brunswick, NJ 08901, NDC 42913-020-00, UPC 815195014097
Brand
A.P. Deauville, LLC
Lot Codes / Batch Numbers
Lot #: 070421E211, 070921E221, 071021E231, 071021E241, Exp 7/2021
Products Sold
Lot #: 070421E211; 070921E221; 071021E231; 071021E241, Exp 7/2021
A.P. Deauville, LLC is recalling Soft Whisper by Powerstick Dandruff Shampoo (Pyrithione Zinc), 14.4 FL OZ. (426 mL), A.P. Deauville due to cGMP Deviations: Soft Whisper Dandruff Shampoo was produced with water that failed USP specifications.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA drug enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
cGMP Deviations: Soft Whisper Dandruff Shampoo was produced with water that failed USP specifications.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm, their healthcare provider, or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 7, 2026